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eurological outcome in Polytrauma patient having traumatic brain injury coming for non neurosurgery under BIS and Non-BIS guided anaesthesia : A Randomised Controlled Study.

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/07/055403
Lead Sponsor
Department of Anaesthesia and Intensive Care
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Polytrauma patient with Traumatic brain injury of age 18-60 year coming for emergency non neurological surgery in less than 7 days post injury.

2.Patients or their relatives giving consent to participate in the study

Exclusion Criteria

1.Polytrauma patient not within the described age limit.

2.Baseline BIS value less than 60

3.Forehead injury where BIS monitor cannot be placed.

4.Perioperative hypothermia.

5.Dyselectrolytemia.

6.Patients not requiring general anaesthesia.

7.Patients or relatives not giving consent

8.Pregnant patient

9.Spine surgery

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess postoperative neurological outcome by using FOUR score between BIS guided & non-BIS guided anaesthesia depth monitoring in Traumatic brain injury patient undergoing emergency non neurosurgical surgery.Timepoint: 72 hours postsurgery
Secondary Outcome Measures
NameTimeMethod
To compare FOUR score & GCS post-surgery. <br/ ><br> To compare GOS-E. <br/ ><br>Timepoint: FOUR Score & GCS at 24hours postsurgery. <br/ ><br> <br/ ><br>GOS-E after 3months postsurgery telephonically <br/ ><br>
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